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Journal articles on the topic 'Absolute configuration'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

Flack, H. D., and G. Bernardinelli. "Absolute structure and absolute configuration." Acta Crystallographica Section A Foundations of Crystallography 55, no. 5 (1999): 908–15. http://dx.doi.org/10.1107/s0108767399004262.

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Fundamental notions concerning absolute structure and absolute configuration, and their determination from single-crystal diffraction measurements, are presented and reviewed. A glossary of terms with definitions useful in this field is provided. For absolute structure and its determination, the separate but interacting influences of the structure and the inversion-distinguishing power of an X-ray diffraction experiment with dispersive scatterers are examined. Important experimental and algorithmic details of the current methods used for absolute-structure determination are provided. Character

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2

Bunting, John W. "Assigning absolute configuration." Journal of Chemical Education 64, no. 8 (1987): 731. http://dx.doi.org/10.1021/ed064p731.2.

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3

Krupa, Johann, Helmut Lackner, Peter G. Jones, Karen Schmidt-Bäse, and George M. Sheldrick. "Die absolute Konfiguration der Juglomycine/The Absolute Configuration of the Juglomycins." Zeitschrift für Naturforschung B 44, no. 3 (1989): 345–52. http://dx.doi.org/10.1515/znb-1989-0316.

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The absolute configurations of the known juglomycins A (1) and B (2) have been elucidated by single crystal X-ray structure analysis of 1 and its 6,8-dibromo derivative (1b). The structure of 2 has been corrected; it differs from 1 in its configuration at C-4', and not at C-3' as previously assumed. Relationships with the closely related isochromanquinone antibiotics are discussed.

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4

Flack, H. D., and G. Bernardinelli. "ChemInform Abstract: Absolute Structure and Absolute Configuration." ChemInform 31, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.200006295.

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5

YAMAGUCHI, Kentaro, Yukiko MAKINO, Yasuteru URANO, and Tetsuo NAGANO. "Absolute Configuration of Cathine." Analytical Sciences 15, no. 10 (1999): 1039–40. http://dx.doi.org/10.2116/analsci.15.1039.

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6

Saito, Shoichi, Natsuki Tanaka, Katsumi Fujimoto, and Hiroshi Kogen. "Absolute Configuration of Scyphostatin." Organic Letters 2, no. 4 (2000): 505–6. http://dx.doi.org/10.1021/ol991351p.

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7

Bats, J. W., and S. H. Öhlinger. "Absolute configuration of isocurcumenol." Acta Crystallographica Section C Crystal Structure Communications 55, no. 9 (1999): 1595–98. http://dx.doi.org/10.1107/s0108270199006101.

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8

Fun, Hoong-Kun, Suchada Chantrapromma, Orapun Yodsaoue, and Chatchanok Karalai. "Absolute configuration of odorine." Acta Crystallographica Section E Structure Reports Online 66, no. 9 (2010): o2437—o2438. http://dx.doi.org/10.1107/s1600536810034227.

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9

Shimizu, Yuzuru, Hideo Bando, Hong-Nong Chou, Gregory Van Duyne, and Jon C. Clardy. "Absolute configuration of brevetoxins." Journal of the Chemical Society, Chemical Communications, no. 22 (1986): 1656. http://dx.doi.org/10.1039/c39860001656.

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10

Fun, Hoong-Kun, Nantiya Joycharat, Supayang Piyawan Voravuthikunchai, and Suchada Chantrapromma. "Absolute configuration of isoeichlerialactone." Acta Crystallographica Section E Structure Reports Online 66, no. 4 (2010): o879—o880. http://dx.doi.org/10.1107/s1600536810009499.

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11

Caro, Miguel S. B., Leonardo H. de Oliveira, Vinicius Ilha, Robert A. Burrow, Ionara I. Dalcol, and Ademir F. Morel. "Absolute Configuration of Franganine." Journal of Natural Products 75, no. 6 (2012): 1220–22. http://dx.doi.org/10.1021/np300206x.

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12

Huang, Liang, Yi-Kang Si, Günther Snatzke, Duo-Kai Zheng, and Jin Zhou. "Absolute configuration of gossypol." Collection of Czechoslovak Chemical Communications 53, no. 11 (1988): 2664–66. http://dx.doi.org/10.1135/cccc19882664.

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13

Mitchell, Robin E., Michael C. Pirrung, and Gerard M. McGeehan. "Absolute configuration of norcoronatine." Phytochemistry 26, no. 10 (1987): 2695–97. http://dx.doi.org/10.1016/s0031-9422(00)83574-8.

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14

Fun, Hoong-Kun, Ittipon Siridechakorn, Surat Laphookhieo, and Suchada Chantrapromma. "Absolute configuration of micromelin." Acta Crystallographica Section E Structure Reports Online 67, no. 7 (2011): o1706—o1707. http://dx.doi.org/10.1107/s1600536811022720.

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15

Polavarapu, P. L., A. L. Cholli, and G. Vernice. "Absolute configuration of isoflurane." Journal of the American Chemical Society 114, no. 27 (1992): 10953–55. http://dx.doi.org/10.1021/ja00053a038.

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16

Jiang, Ren-Wang, Wencai Ye, Pang-Chui Shaw, Paul Pui-Hay But, and Thomas C. W. Mak. "Absolute configuration of neostenine." Journal of Molecular Structure 966, no. 1-3 (2010): 18–22. http://dx.doi.org/10.1016/j.molstruc.2009.11.059.

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17

Adio, Adewale Martins, Claudia Paul, Hailemichael Tesso, Petra Kloth, and Wilfried A. König. "Absolute configuration of helminthogermacrene." Tetrahedron: Asymmetry 15, no. 10 (2004): 1631–35. http://dx.doi.org/10.1016/j.tetasy.2004.03.030.

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18

Shibata, Tomoyuki, Shinwa Kurihara, Keiko Yoda, and Hideyuki Haruyama. "Absolute configuration of leustroducsins." Tetrahedron 51, no. 44 (1995): 11999–2012. http://dx.doi.org/10.1016/0040-4020(95)00759-2.

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19

Koehler, K. F., H. Zaddach, A. D. Kuntsevich, I. I. Chervin, and R. G. Kostyanovsky. "Absolute configuration of somane." Russian Chemical Bulletin 42, no. 9 (1993): 1611–12. http://dx.doi.org/10.1007/bf00699210.

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20

Archelas, A., та R. Furstoss. "Absolute Configuration of α-Methylstyrene Oxide: The Correct Absolute Configuration/Optical Rotation Correlation". Journal of Organic Chemistry 64, № 16 (1999): 6112–14. http://dx.doi.org/10.1021/jo990474k.

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21

Pedras, M. Soledade C. "Determination of the absolute configuration of the fragments composing the phytotoxin phomalide." Canadian Journal of Chemistry 75, no. 3 (1997): 314–17. http://dx.doi.org/10.1139/v97-035.

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The absolute configurations of the residues constituting phomalide (1) were determined on the products resulting from acidic hydrolysis. The configurations of the amino acids Val and Leu were determined as (S) and (R), respectively, by chiral GC analysis (Chirasil-Val capillary column), employing N-trifluoroacetyl (TFA) amino acid methyl ester derivatives. The configurations of the hydroxy acids O-Phe and O-Leu were determined as (S) by 1H NMR of the Mosher's esters of the isopropyl ester derivatives. The method described allowed for the unambiguous assignment of the absolute configuration of

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22

BRITO, IVÁN, JORGE BORQUEZ, EMILY HUAROTE, LUIS LOYOLA, ALEJANDRO CÁRDENAS, and MARIO SIMIRGIOTIS. "ABSOLUTE CONFIGURATION OF MULINOLIC ACID." Journal of the Chilean Chemical Society 62, no. 3 (2017): 3658–60. http://dx.doi.org/10.4067/s0717-97072017000303658.

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23

Hanaoka, Miyoji, Kazuyoshi Nagami, and Shingo Yasuda. "The Absolute Configuration of (+)-Canadaline." HETEROCYCLES 29, no. 2 (1989): 221. http://dx.doi.org/10.3987/com-89-4792.

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24

Fun, Hoong-Kun, Abdul Wahab Salae, Ibrahim Abdul Razak, Melati Khairuddean, and Suchada Chantrapromma. "Absolute configuration of fibaruretin B." Acta Crystallographica Section E Structure Reports Online 67, no. 5 (2011): o1246—o1247. http://dx.doi.org/10.1107/s1600536811014887.

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25

Rodríguez, M. L., J. D. Martín, and D. Estrada. "The absolute configuration of (+)-isoconcinndiol." Acta Crystallographica Section C Crystal Structure Communications 45, no. 2 (1989): 306–8. http://dx.doi.org/10.1107/s0108270188010947.

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26

Godfrey, R., R. Hargreaves, and P. B. Hitchcock. "Absolute configuration of (+)-ethambutol hydrobromide." Acta Crystallographica Section C Crystal Structure Communications 48, no. 1 (1992): 79–81. http://dx.doi.org/10.1107/s0108270191004274.

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27

Fun, Hoong-Kun, Nantiya Joycharat, Supayang Piyawan Voravuthikunchai, and Suchada Chantrapromma. "Absolute configuration of methyl isoeichlerialactone." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1604—o1605. http://dx.doi.org/10.1107/s1600536810018295.

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28

Aliev, Abil’ E., Anna A. Sinitsyna, Anatolii I. Bokanov, Pavel Yu Ivanov, Vasilii I. Shvedov, and Remir G. Kostyanovskii. "The Absolute Configuration of Pyrazidole." Mendeleev Communications 2, no. 4 (1992): 130–31. http://dx.doi.org/10.1070/mc1992v002n04abeh000168.

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29

Castro, Rosane de P., Carolina da S. Matos, Cláudia A. do Nascimento, et al. "Absolute configuration of strictosidinic acid." Acta Crystallographica Section C Crystal Structure Communications 68, no. 4 (2012): m94—m96. http://dx.doi.org/10.1107/s0108270112010372.

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The absolute configuration of strictosidinic acid, (2S,3R,4S)-3-ethenyl-2-(β-D-glucopyranosyloxy)-4-{[(1S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl]methyl}-3,4-dihydro-2H-pyran-5-carboxylate, was determined from its sodium chloride trihydrate, poly[[diaqua((2S,3R,4S)-3-ethenyl-2-(β-D-glucopyranosyloxy)-4-{[(1S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-1-yl]methyl}-3,4-dihydro-2H-pyran-5-carboxylate)sodium] chloride monohydrate], {[Na(C26H32N2O9)(H2O)2]Cl·H2O}n. The strictosidinic acid molecule participates in intermolecular hydrogen bonds of the O—H...O and O—H...Cl types. The solid

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30

Mattern, Daniell Lewis. "Fingertip assignment of absolute configuration." Journal of Chemical Education 62, no. 3 (1985): 191. http://dx.doi.org/10.1021/ed062p191.

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31

Hambly, Gordon F. "Assigning absolute configuration: Another view." Journal of Chemical Education 64, no. 8 (1987): 732. http://dx.doi.org/10.1021/ed064p732.1.

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32

Lange, Joachim, Gerd Benirschke, and Hans Achenbach. "The absolute configuration of assufulvenal." Phytochemistry 45, no. 2 (1997): 349–52. http://dx.doi.org/10.1016/s0031-9422(96)00798-4.

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33

Bringmann, Gerhard, Matthias Reichert, and Yasmin Hemberger. "The absolute configuration of streptonigrin." Tetrahedron 64, no. 3 (2008): 515–21. http://dx.doi.org/10.1016/j.tet.2007.11.015.

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34

Hirai, Nobuhiro, Masahiko Okamoto, Hiroaki Udagawa, Munehiro Yamamuro, Masayoshi Kato, and Koichi Koshimizu. "Absolute Configuration of Dehydrodiconiferyl Alcohol." Bioscience, Biotechnology, and Biochemistry 58, no. 9 (1994): 1679–84. http://dx.doi.org/10.1271/bbb.58.1679.

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35

Sanhueza, Carlos A., Ander C. Arias, Rosa L. Dorta, and Jesús T. Vázquez. "Absolute configuration of glycosyl sulfoxides." Tetrahedron: Asymmetry 21, no. 15 (2010): 1830–32. http://dx.doi.org/10.1016/j.tetasy.2010.06.019.

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36

White, James D., Todd C. Somers, and G. Nagabushana Reddy. "The absolute configuration of (-)-botryococcene." Journal of the American Chemical Society 108, no. 17 (1986): 5352–53. http://dx.doi.org/10.1021/ja00277a054.

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37

Saito, Fumito, Dennis Gerbig, Jonathan Becker, and Peter R. Schreiner. "Absolute Configuration of trans-Perhydroazulene." Organic Letters 22, no. 10 (2020): 3895–99. http://dx.doi.org/10.1021/acs.orglett.0c01184.

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38

Ichihara, Akitami, Masayoshi Miki, and Sadao Sakamura. "Absolute configuration of (−)-solanapyrone A." Tetrahedron Letters 26, no. 20 (1985): 2453–54. http://dx.doi.org/10.1016/s0040-4039(00)94851-2.

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39

Fun, Hoong-Kun, Cholpisut Tantapakul, Surat Laphookhieo, Nawong Boonnak, and Suchada Chantrapromma. "Absolute configuration of xerophenone A." Acta Crystallographica Section E Structure Reports Online 68, no. 5 (2012): o1451—o1452. http://dx.doi.org/10.1107/s1600536812015267.

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40

Shing, Tony K. M. "Oblongolide: synthesis and absolute configuration." Journal of the Chemical Society, Chemical Communications, no. 1 (1986): 49. http://dx.doi.org/10.1039/c39860000049.

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41

Iwai, Takahiro, Takaaki Kubota, and Jun’ichi Kobayashi. "Absolute Configuration of Amphidinin A." Journal of Natural Products 77, no. 6 (2014): 1541–44. http://dx.doi.org/10.1021/np5003065.

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42

Suzuki, Minoru, Kazuya Kurata, Teruaki Suzuki, and Etsuro Kurosawa. "The Absolute Configuration of Isoprelaurefucin." Bulletin of the Chemical Society of Japan 59, no. 9 (1986): 2953–55. http://dx.doi.org/10.1246/bcsj.59.2953.

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43

Shing, Tony K. M., and Hon-chung Tsui. "Goniofufurone: synthesis and absolute configuration." Journal of the Chemical Society, Chemical Communications, no. 5 (1992): 432. http://dx.doi.org/10.1039/c39920000432.

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44

Fun, Hoong-Kun, Orapun Yodsaoue, Chatchanok Karalai, and Suchada Chantrapromma. "Absolute configuration of isovouacapenol C." Acta Crystallographica Section E Structure Reports Online 66, no. 8 (2010): o2059—o2060. http://dx.doi.org/10.1107/s1600536810028023.

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45

Satake, Masayuki, Akio Morohashi, Hiroki Oguri, et al. "The Absolute Configuration of Ciguatoxin." Journal of the American Chemical Society 119, no. 46 (1997): 11325–26. http://dx.doi.org/10.1021/ja972482t.

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46

Weckert, Edgar, Kurt Hümmer, Ivan Addae-Mensah, and H. Achenbach. "The absolute configuration of chiromodine." Phytochemistry 31, no. 6 (1992): 2170–72. http://dx.doi.org/10.1016/0031-9422(92)80393-s.

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47

Aakermann, Torunn, and Synnøve Liaaen-Jensen. "Pyrrhoxanthin, reisolation and absolute configuration." Phytochemistry 31, no. 5 (1992): 1779–82. http://dx.doi.org/10.1016/0031-9422(92)83146-p.

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48

Kim, Jin-Woong, Sang-Sup Jew, Youn-Sang Cho, and Chae-Ho Cook. "The absolute configuration of ketoprofen." Archives of Pharmacal Research 10, no. 1 (1987): 25–28. http://dx.doi.org/10.1007/bf02855617.

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49

Dahmann, Georg, and Reinhard W. Hoffmann. "The Absolute Configuration of Muamvatin." Liebigs Annalen der Chemie 1994, no. 8 (1994): 837–45. http://dx.doi.org/10.1002/jlac.199419940813.

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50

Beyerman, H. C., L. Maat, and M. P. Hegarty. "The absolute configuration of mimosine." Recueil des Travaux Chimiques des Pays-Bas 83, no. 10 (2010): 1078–82. http://dx.doi.org/10.1002/recl.19640831011.

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